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7. [Transmission of a neurologic degeneration in a family for 4 generations manifested under variable semiologic aspects (pure pyramidal, pure cerebello-pyramidal involvement or involvement with abolition of reflexes and severe sensory disorders]. Mettey R, Hoppeler A, Gil R. J Genet Hum; 1981 Sep; 29(3):227-34. PubMed ID: 7334346 [No Abstract] [Full Text] [Related]
13. [Family with hereditary polyneuropthy assoicated with pyramidal signs]. Doi H, Shibasaki H, Goto I, Kuroiwa Y, Ohta M. Rinsho Shinkeigaku; 1976 Sep; 16(9):642-8. PubMed ID: 1034548 [No Abstract] [Full Text] [Related]
14. [2 autopsy cases of the spinocerebellar degeneration with cerebral atrophy]. Kato Y, Takayama K, Tsujiyama Y, Kaga T, Satowa H. No To Shinkei; 1970 Oct; 22(10):1201-8. PubMed ID: 5536190 [No Abstract] [Full Text] [Related]
15. [Amyotrophic form of a spinocerebellar degeneration. Anatomoclinical study and nosological discussion]. Boudouresques J, Toga M, Khalil R, Gosset A, Vigouroux RA, Pellissier JF. Rev Neurol (Paris); 1971 Jul; 125(1):25-38. PubMed ID: 5138162 [No Abstract] [Full Text] [Related]
16. A simple method for evoking dorsiflexion of the hallux in pyramidal lesions. Serbănescu T. Rev Roum Neurol Psychiatr; 1974 Jul; 11(3):219-25. PubMed ID: 4846957 [No Abstract] [Full Text] [Related]